Aleph-4

Salts []
2,5-Dimethoxy-4-isopropylthioamphetamine hydrochloride

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C14H23NO2S[1]
Molecular mass	269.40 g/mol[1]
Predicted LogP	3[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	1-(2,5-dimethoxy-4-propan-2-ylsulfanylphenyl)propan-2-amine[1]
SMILES	CC(C)SC1=C(C=C(C(=C1)OC)CC(C)N)OC[1]
InChI	InChI=1S/C14H23NO2S/c1-9(2)18-14-8-12(16-4)11(6-10(3)15)7-13(14)17-5/h7-10H,6,15H2,1-5H3[1]
InChIKey	BCWCXWKCQMBFBQ-UHFFFAOYSA-N[1]

Dosing

2,5-Dimethoxy-4-isopropylthioamphetamine

2,5-Dimethoxy-4-isopropylthioamphetamine (also known as 2,5-Dimethoxy-4-iso-propylthioamphetamine, 1-(2,5-Dimethoxy-4-i-propylthiophenyl)-2-aminopropane, J273.479F, 1-[2,5-dimethoxy-4-(propan-2-ylsulfanyl)phenyl]propan-2-amine, YEA64326, 2,5-Dimethoxy-α-methyl-4-((1-methylethyl)thio)benzeneethanamine, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-((1-methylethyl)thio)-, HY-138095 or 2-(4-Isopropylsulfanyl-2,5-dimethoxy-phenyl)-1-methyl-ethylamine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

2,5-Dimethoxy-4-isopropylthioamphetamine is typically found in the form of its hydrochloride salt.

Stereochemistry

(RS)-2,5-Dimethoxy-4-isopropylthioamphetamine is a racemic mixture of the optical stereoisomers

See also

• 2,5-Dimethoxyphenethylamine
• Substituted 2,5-dimethoxyphenethylamines
• Anodyne

External links

• 2,5-Dimethoxy-4-isopropylthioamphetamine (Wikidata)
• 2,5-Dimethoxy-4-isopropylthioamphetamine (PubChem)
• 2,5-Dimethoxy-4-isopropylthioamphetamine (ChEMBL)
• 2,5-Dimethoxy-4-isopropylthioamphetamine (Common Chemistry)
• 2,5-Dimethoxy-4-isopropylthioamphetamine (UNII)
• 2,5-Dimethoxy-4-isopropylthioamphetamine (EPA DSSTox)

References